Table 4.
Publication | Patient population | Endpoints/definition of CIN | Study type | Sponsor | Procedure | Statistical sample power |
---|---|---|---|---|---|---|
Carraro et al. [32] | Patients with mild to moderate CRI | SCr ≥50% 24 h after administration | Prospective, randomized Double-blinded | Investigator | i.v. urography | 80% N=64 |
Chuang et al. [33] | Patients with CRI and/or diabetes | SCr ≥25% 72 h after administration | Prospective, randomized Double-blinded | Investigator | i.v. urography | Not available N=50 |
Barrett et al. [34] | Patients with moderate to severe CRI | SCr ≥0.5 mg/dL and/or SCr ≥25% 2–2 days after administration | Prospective, randomized Double-blinded | Bracco | CT | Not available N=153 |
Thomsen et al. [35] | Patients with moderate to severe CRI | SCr ≥0.5 mg/dL 24, 48 amd 72 h after administration | Prospective, randomized Double-blinded | Bracco | CT | Not available N=184 |
Nguyen et al. [36] | Patients with moderate to severe CRI | SCr ≥0.5 mg/dL 24, 48 and 72 h after administration | Prospective, randomized Double-blinded | GEHC | CT | 95% N=117 |
Kuhn et al. [37] | Patients with moderate to severe CRI | SCr ≥25% 48–72 h after administration | Prospective, randomized Double-blinded | Bracco | CT | Not available N=248 |
Zo’o et al. [38] | Pediatric patients (aged 1–16) with normal renal function | SCr ≥0.5 mg/dL 48–72 h after administration | Prospective, randomized Double-blinded | Guerbet | CT | 80% N=146 |